arXiv subjects

Enrique Burzurí

Publications and source records attributed to Enrique Burzurí.

10 recordsLinked to original sources

arXiv2026

Electrical Probing of Sub-Néel Spin Dynamics in Two-Dimensional Antiferromagnets Using Graphene Heterostructures

Low-dimensional antiferromagnetic van der Waals materials have emerged as a versatile platform for exploring exotic spin dynamics and magnetic phases, yet electrically accessing these phenomena remains a major challenge because of their vanishing net magnetization and highly insulating nature. Here, we demonstrate that graphene can act as an ultrasensitive electrical transducer of hidden spin dynamics in two-dimensional antiferromagnets. By integrating graphene with the van der Waals antiferromagnet FePS$_3$, low-temperature transport measurements combined with magnetic-field and gate-voltage control reveal multiple resistance anomalies well below the Néel temperature. Their distinct temperature, magnetic-field, and carrier-density dependences enable us to associate these anomalies with magnon excitations and with a low-temperature magnetic reconfiguration of the antiferromagnetic state, both of which remain largely inaccessible to conventional magnetometry. Density functional theory calculations further show that competing antiferromagnetic spin configurations in FePS$_3$ are nearly degenerate in energy while producing markedly different electronic responses in the adjacent graphene layer. The pronounced electrostatic tunability of these signatures demonstrates that graphene directly transduces interfacial magnetic dynamics into an electrical signal. Our work establishes graphene/antiferromagnetic van der Waals heterostructures as a versatile platform for the electrical readout of spin dynamics in two-dimensional magnets.

cond-mat.mtrl-sci↗

arXiv2026

Physically Unclonable Functions Based on Single-Walled Carbon Nanotubes: A Scalable and Inexpensive Method toward Unique Identifiers

A physically un-clonable function (PUF) is a physical system that cannot be reproduced or predicted and therefore is a good basis to build security and anti-counterfeiting applications. The unclonability of PUFs typically stems from the randmoness induced in a system during sophisticated fabrication methods. It is precisely this built-in complexity the bottleneck hindering scalability and increasing costs. Here, we produce in a simple manner PUFs based on arrays of carbon nanotubes junctions simultaneously assembled by dielectrophoresis. We demonstrate that the intrinsic inhomogeneity of carbon nanotubes at the nanoscale, combined with the unpredictability introduced by liquid phase-based fabrication methods results in unique electronic profiles of easily scalable devices. This approach could be extrapolated to generate PUFs based on other nanoscale materials

cond-mat.mtrl-sci↗

arXiv2026

Molecular-based coordination polymer as reversible and precise acetonitrile electro-optical readout

Efficient detection of harmful organic volatile compounds is a major health and environmental need in industrialized societies. Tailor-made metal-organic frameworks and other coordination polymers are emerging as promising sensing molecular materials thanks to their responsivity to a wide variety of external stimuli, and could be used to complement conventional sensors. Here, a non-porous crystalline 1D Fe(II) coordination polymer acting as a porous acetonitrile host is presented. The desorption of interstitial acetonitrile is accompanied by magneto-structural transitions easily detectable in the optical and electronic properties of the material. The structural switch and therefore its (opto)electronic readout are reversible under exposition of the crystal to acetonitrile vapor. Coordination polymers can be versatile sensors for volatile acetonitrile and potentially other organic compounds.

cond-mat.mtrl-sci↗

arXiv2019

Mechanical and liquid phase exfoliation of cylindrite: a natural van der Waals superlattice with intrinsic magnetic interactions

We report the isolation of thin flakes of cylindrite, a naturally occurring van der Waals superlattice, by means of mechanical and liquid phase exfoliation. We find that this material is a heavily doped p-type semiconductor with a narrow gap (<0.85 eV) with intrinsic magnetic interactions that are preserved even in the exfoliated nanosheets. Due to its environmental stability and high electrical conductivity, cylindrite can be an interesting alternative to the existing two-dimensional magnetic materials.

physics.app-ph↗

arXiv2018

Robust organic radical molecular junctions using acetylene terminated groups for C-Au bond formation

Organic paramagnetic and electroactive molecules are attracting interest as core components of molecular electronic and spintronic devices. Currently, further progress is hindered by the modest stability and reproducibility of the molecule/electrode contact. We report the synthesis of a persistent organic radical bearing one and two terminal alkyne groups to form Au-C σ bonds. The formation and stability of self-assembled monolayers and the electron transport through single-molecule junctions at room temperature have been studied. The combined analysis of both systems demonstrates that this linker forms a robust covalent bond with gold and a better-defined contact when compared to traditional sulfur-based linkers. Density functional theory and quantum transport calculations support the experimental observation highlighting a reduced variability of conductance values for the C-Au based junction. Our findings advance the quest for robustness and reproducibility of devices based on electroactive molecules.

cond-mat.mes-hall↗

arXiv2018

Redox-Induced Gating of the Exchange Interactions in a Single Organic Diradical

Embedding a magnetic electroactive molecule in a three-terminal junction allows for the fast and local electric field control of magnetic properties desirable in spintronic devices and quantum gates. Here, we provide an example of this control through the reversible and stable charging of a single all-organic neutral diradical molecule. By means of inelastic electron tunnel spectroscopy (IETS) we show that the added electron occupies a molecular orbital distinct from those containing the two radical electrons, forming a spin system with three antiferromagnetically-coupled spins. Changing the redox state of the molecule therefore switches on and off a parallel exchange path between the two radical spins through the added electron. This electrically-controlled gating of the intramolecular magnetic interactions constitutes an essential ingredient of a single-molecule $\sqrt{\text{SWAP}}$ quantum gate.

cond-mat.mes-hall↗

arXiv2018

Spin-State dependent Conductance Switching in Single Molecule-Graphene Junctions

Spin-crossover (SCO) molecules are versatile magnetic switches with applications in molecular electronics and spintronics. Downscaling devices to the single-molecule level remains, however, a challenging task since the switching mechanism in bulk is mediated by cooperative intermolecular interactions. Here, we report on electron transport through individual Fe-SCO molecules coupled to few-layer graphene electrodes \textit{via} $π- π$ stacking. We observe a distinct bistability in the conductance of the molecule and a careful comparison with density functional theory (DFT) calculations allows to associate the bistability with a SCO-induced orbital reconfiguration of the molecule. We find long spin-state lifetimes that are caused by the specific coordination of the magnetic core and the absence of intermolecular interactions according to our calculations. In contrast with bulk samples, the SCO transition is not triggered by temperature but induced by small perturbations in the molecule at any temperature. We propose plausible mechanisms that could trigger the SCO at the single-molecule level.

cond-mat.mes-hall↗

arXiv2018

Simultaneous Assembly of van der Waals Heterostructures into Multiple Nanodevices

Van der Waals heterostructures (vdWH) are made of different two-dimensional (2D) layers stacked on top of each other, forming a single material with unique properties that differ from those of the individual 2D constituent layers, and that can be modulated through the interlayer interaction. These hetero-materials can be artificially made by mechanical stamping, solution processing or epitaxial growth. Alternatively, franckeite has been recently described as an example of a naturally-occurring vdWH that can be exfoliated down to nanometer thicknesses. Research on vdWHs has so far been limited to manually exfoliated and stamped individual devices. Here, a scalable and fast method to fabricate vdWH nanodevices from liquid phase exfoliated nanoflakes is reported. The transport and positioning of the flakes into localized submicrometer structures is achieved simultaneously in multiple devices via a dielectrophoretic process. The complex vdWH is preserved after dielectrophoresis and the properties of the resulting field-effect transistors are equivalent to those fabricated via mechanical exfoliation and stamping. The combination of liquid phase exfoliation and dielectrophoretic assembly is particularly suited for the study of vdWHs and applications where large-scale fabrication is required.

cond-mat.mtrl-sci↗

arXiv2017

Quantum-enhanced Landauer erasure and storage

The erasure of a bit of information encoded in a physical system is an irreversible operation bound to dissipate an amount of energy $Q = k_\text{B} T\ln 2$. As a result, work $W \geq Q$ has to be applied to the physical system to restore the erased information content. This limit, called Landauer limit, sets a minimal energy dissipation inherent to any classical computation. In the pursuit of the fastest and most efficient means of computation, the ultimate challenge is to produce a memory device executing an operation as close to this limit in the shortest time possible. Here, we use a crystal of molecular nanomagnets as a spin-memory device and measure the work needed to carry out a storage operation. Exploiting a form of quantum annealing, we border the Landauer limit while preserving fast operation. Owing to the tunable and fast dynamics of this process, the performance of our device in terms of energy-time cost is orders of magnitude better than existing memory devices to date. This result suggests a way to enhance classical computations by using quantum processes.

quant-ph↗

arXiv2016

Transport mirages in single-molecule devices

Molecular systems can exhibit a complex, chemically tailorable inner structure which allows for targeting of specific mechanical, electronic and optical properties. At the single-molecule level, two major complementary ways to explore these properties are molecular quantum-dot structures and scanning probes. This article outlines comprehensive principles of electron-transport spectroscopy relevant to both these approaches and presents a new, high-resolution experiment on a high-spin single-molecule junction exemplifying these principles. Such spectroscopy plays a key role in further advancing our understanding of molecular and atomic systems, in particular the relaxation of their spin. In this joint experimental and theoretical analysis, particular focus is put on the crossover between resonant regime [single-electron tunneling (SET)] and the off-resonant regime [inelastic electron (co)tunneling (IETS)]. We show that the interplay of these two processes leads to unexpected mirages of resonances not captured by either of the two pictures alone. Although this turns out to be important in a large fraction of the possible regimes of level positions and bias voltages, it has been given little attention in molecular transport studies. Combined with nonequilibrium IETS -- four-electron pump-probe excitations -- these mirages provide crucial information on the relaxation of spin excitations. Our encompassing physical picture is supported by a master-equation approach that goes beyond weak coupling. The present work encourages the development of a broader connection between the fields of molecular quantum-dot and scanning probe spectroscopy.

cond-mat.mes-hall↗